Autosomal recessive dopa-responsive dystonia (Q64260): Difference between revisions
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Este é um raro transtorno hereditário recessivo do movimento que geralmente se manifesta durante a primeira infância. As características clínicas são como na categoria parental. Pode ser devido a uma mutação no gene da tirosina hidroxilase e tem um fenótipo mais complexo do que a mutação da GTP ciclo-hidrolase. Podem ocorrer crises oculogíricas. | |||||||||||||||
| description / en | description / en | ||||||||||||||
This is a rare recessively inherited movement disorder which usually manifests itself during early childhood. The characteristic clinical features are as in the parent category. It may be is due to a mutation in thetyrosine hydroxylase gene and has a more complex phenotype than GTP cyclohydrolase mutation. Oculogyric crises may occur. | |||||||||||||||
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| Property / Canonical URI: https://id.who.int/icd/entity/1208668939 / rank | |||||||||||||||
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CID11:ID_1208668939 | |||||||||||||||
| Property / CURIE: CID11:ID_1208668939 / rank | |||||||||||||||
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dki-india-ID_1208668939 | |||||||||||||||
| Property / Canary Token: dki-india-ID_1208668939 / rank | |||||||||||||||
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Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
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| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
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13 August 2026
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| Property / Collection date: 13 August 2026 / rank | |||||||||||||||
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Latest revision as of 11:51, 14 August 2026
This is a rare recessively inherited movement disorder which usually manifests itself during early childhood. The characteristic clinical features are as in the parent category. It may be is due to a mutation in thetyrosine hydroxylase gene and has a more complex phenotype than GTP cyclohydrolase mutation. Oculogyric crises may occur.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_1208668939 |
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| English | Autosomal recessive dopa-responsive dystonia |
This is a rare recessively inherited movement disorder which usually manifests itself during early childhood. The characteristic clinical features are as in the parent category. It may be is due to a mutation in thetyrosine hydroxylase gene and has a more complex phenotype than GTP cyclohydrolase mutation. Oculogyric crises may occur. |
Statements
CID11:ID_1208668939
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dki-india-ID_1208668939
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Concluído
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13 August 2026
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